المؤلفون: Sokolova D., Piccini G., Tiefenbacher K.

المساهمون: Sokolova, D., Piccini, G., Tiefenbacher, K.

مصطلحات موضوعية: Chiral Self-Assemblie, Enantioselective Catalysi, Resorcinarene Capsule, Supramolecular Catalysi, Terpene Cyclization

Relation: info:eu-repo/semantics/altIdentifier/pmid/35324038; info:eu-repo/semantics/altIdentifier/wos/WOS:000784802800001; volume:61; issue:25; firstpage:1; lastpage:5; journal:ANGEWANDTE CHEMIE. INTERNATIONAL EDITION; https://hdl.handle.net/11380/1330548; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85128532033

الاتاحة: https://hdl.handle.net/11380/1330548
https://doi.org/10.1002/anie.202203384

المؤلفون: Fabian Herbrik, Sergio Rossi, Miguel Sanz, Alessandra Puglisi, Maurizio Benaglia

المساهمون: F. Herbrik, S. Rossi, M. Sanz, A. Puglisi, M. Benaglia

مصطلحات موضوعية: catalytic reactor, enantioselective catalysi, flow chemistry, photooxidation, supported catalyst, Settore CHIM/06 - Chimica Organica

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000824422200001; volume:14; issue:17; firstpage:1; lastpage:7; numberofpages:7; journal:CHEMCATCHEM; https://hdl.handle.net/2434/945971; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85134214936

الاتاحة: https://hdl.handle.net/2434/945971
https://doi.org/10.1002/cctc.202200461

المؤلفون: Herbrik, Fabian, Sanz, Miguel, Puglisi, Alessandra, Rossi, Sergio, Benaglia, Maurizio

المساهمون: F. Herbrik, M. Sanz, A. Puglisi, S. Rossi, M. Benaglia

مصطلحات موضوعية: chiral API, enantioselective catalysi, flow chemistry, organophotoredox catalysi, telescoped proce, Settore CHIM/06 - Chimica Organica

Relation: info:eu-repo/semantics/altIdentifier/pmid/35239197; info:eu-repo/semantics/altIdentifier/wos/WOS:000790437300001; volume:28; issue:33; firstpage:1; lastpage:7; numberofpages:7; journal:CHEMISTRY-A EUROPEAN JOURNAL; http://hdl.handle.net/2434/915172; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85129304323

الاتاحة: http://hdl.handle.net/2434/915172
https://doi.org/10.1002/chem.202200164

المؤلفون: Lonardi G., Franco S., Sartorello M., De Faveri C., Stivanello M., Licini G., Orlandi M.

المساهمون: Lonardi, G., Franco, S., Sartorello, M., De Faveri, C., Stivanello, M., Licini, G., Orlandi, M.

مصطلحات موضوعية: CuH-catalysi, enantioselective catalysi, hydrocupration, olefinhydroalkylation, cyclopropanes

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:001230109100001; volume:14; issue:11; firstpage:8730; lastpage:8738; numberofpages:9; journal:ACS CATALYSIS; https://hdl.handle.net/11577/3522922; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85194059554

الاتاحة: https://hdl.handle.net/11577/3522922
https://doi.org/10.1021/acscatal.4c02119

المؤلفون: Michalak M., Czerwinski P., Sniady-Maciazek K., Musiol S., Danylyuk O., Wierzbicki M., Tomasini M., Poater A.

المساهمون: Michalak, M., Czerwinski, P., Sniady-Maciazek, K., Musiol, S., Danylyuk, O., Wierzbicki, M., Tomasini, M., Poater, A.

مصطلحات موضوعية: allenol cyclization, enantioselective catalysi, gold(I) complexe, N-heterocyclic carbene ligand

Relation: info:eu-repo/semantics/altIdentifier/pmid/38126930; info:eu-repo/semantics/altIdentifier/wos/WOS:001140912100001; volume:30; issue:13; firstpage:e202303241; lastpage:e202303254; journal:CHEMISTRY-A EUROPEAN JOURNAL; https://hdl.handle.net/11386/4888352

الاتاحة: https://hdl.handle.net/11386/4888352
https://doi.org/10.1002/chem.202303241

المؤلفون: Daniele Ragno, Graziano Di Carmine, Arianna Brandolese, Olga Bortolini, Pier Paolo Giovannini, Alessandro Massi

المساهمون: Ragno, Daniele, DI CARMINE, Graziano, Brandolese, Arianna, Bortolini, Olga, Giovannini, Pier Paolo, Massi, Alessandro

مصطلحات موضوعية: enantioselective catalysi, chiral N-heterocyclic carbene, polystyrene-supported catalyst, flow chemistry, organocatalysis

وصف الملف: ELETTRONICO

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000410005700091; volume:7; issue:9; firstpage:6365; lastpage:6375; numberofpages:11; journal:ACS CATALYSIS; http://hdl.handle.net/11392/2377452; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85029071624

الاتاحة: http://hdl.handle.net/11392/2377452
https://doi.org/10.1021/acscatal.7b02164
https://pubs.acs.org/doi/10.1021/acscatal.7b02164

المؤلفون: Jumde, Ravindra P., MANDOLI, ALESSANDRO

المساهمون: Jumde, Ravindra P., Mandoli, Alessandro

مصطلحات موضوعية: supported organocatalysi, enantioselective catalysi, 2-oxindole, azodicarboxylate, extended recycling

وصف الملف: STAMPA

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000379457300029; volume:6; issue:7; firstpage:4281; lastpage:4285; numberofpages:5; journal:ACS CATALYSIS; http://hdl.handle.net/11568/794952; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84977137233; http://dx.doi.org/10.1021/acscatal.6b01141

الاتاحة: http://hdl.handle.net/11568/794952
https://doi.org/10.1021/acscatal.6b01141

المؤلفون: Orlandi M., Escudero-Casao M., Licini G.

المساهمون: Orlandi, M., Escudero-Casao, M., Licini, G.

مصطلحات موضوعية: aminocatalysi, enantioselective catalysi, tertiary stereocenter, transition-metal catalysi, α-arylation of carbonyl compounds

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000691725500001; volume:53; issue:24; firstpage:4559; lastpage:4566; numberofpages:8; journal:SYNTHESIS; http://hdl.handle.net/11577/3440997; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85114594892

الاتاحة: http://hdl.handle.net/11577/3440997
https://doi.org/10.1055/a-1560-5245

المؤلفون: B. Castano, P. Zardi, Y. C. Hönemann, A. Galarneau, E. Gallo, R. Psaro, A. Caselli, V. Dal Santo

المساهمون: B. Castano, P. Zardi, Y.C. Hönemann, A. Galarneau, E. Gallo, R. Psaro, A. Caselli, V. Dal Santo

مصطلحات موضوعية: Diels-alder reaction, containing macrocyclic ligand, heterogeneous catalyst, asymmetric cyclopropanation, enantioselective catalysi, bis(oxazoline)-copper complexe, mesoporous silica, CU(I) complexe, microporosity, temperature, Settore CHIM/03 - Chimica Generale e Inorganica

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000326056600149; volume:3; issue:44; firstpage:22199; lastpage:22205; numberofpages:7; journal:RSC ADVANCES; http://hdl.handle.net/2434/227297; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84886524564

الاتاحة: http://hdl.handle.net/2434/227297
https://doi.org/10.1039/c3ra44806a

المؤلفون: A. Genoni, M. Benaglia, A. Puglisi, S. Rossi

المساهمون: A. Genoni, M. Benaglia, A. Puglisi, S. Rossi

مصطلحات موضوعية: chiral imine, Diels-Alder reaction, enantioselective catalysi, hydrogen bonding activation, pyridinium salt, Settore CHIM/06 - Chimica Organica

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000291302900015; volume:2011; issue:12; firstpage:1926; lastpage:1929; numberofpages:4; journal:SYNTHESIS; http://hdl.handle.net/2434/165575; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-79958105963

الاتاحة: http://hdl.handle.net/2434/165575
https://doi.org/10.1055/s-0030-1260462

المؤلفون: Hepburn H. B., Magagnano G., Melchiorre P.

المساهمون: Hepburn H.B., Magagnano G., Melchiorre P.

مصطلحات موضوعية: enantioselective catalysi, Mannich-type reaction, organocatalysi, photochemistry, synthetic methods

وصف الملف: STAMPA

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000393231000009; volume:49; issue:1; firstpage:76; lastpage:86; numberofpages:11; journal:SYNTHESIS; info:eu-repo/grantAgreement/EC/H2020/ERC-2015-CoG 681840; https://hdl.handle.net/11585/898158; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84990205066; https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0036-1588606

الاتاحة: https://hdl.handle.net/11585/898158
https://doi.org/10.1055/s-0036-1588606
https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0036-1588606

المؤلفون: SAVOIA, DIEGO, GUALANDI, ANDREA

المساهمون: Autta-ur-Rahman, FRS, Diego Savoia, Andrea Gualandi

مصطلحات موضوعية: Acylic nucleophilic substitution, aldol condensation, alkyne-azide cycloaddition (click reaction), amide, Amine, ASYMMETRIC SYNTHESIS, atkins- richman procedure, aziridine ring opening, bridged macropolycycle, CHIRAL STATIONARY PHASE, CHIRAL PERAZAMACROCYCLES, cyclam, CYCLIZATION, CYCLOPHANE, cyclopolypeptide, enantioselective catalysi, ENANTIOSELECTIVE RECOGNITION, EPOXIDATION, ex-chiral pool synthesi, guanidinium macrocycle, Henry reaction, IMINES, lactamization, METAL COMPLEX, metal ion coordination, mitsunobu reaction, MOLECULAR KNOTS, molecular, MOLECULAR RECOGNITION, MULTICOMPONENT REACTIONS

وصف الملف: ELETTRONICO

Relation: info:eu-repo/semantics/altIdentifier/isbn/9781608050291; info:eu-repo/semantics/altIdentifier/isbn/9781608051151; ispartofbook:Advances in Organic Synthesis Volume # 6; volume:6; firstpage:115; lastpage:166; numberofpages:52; alleditors:Autta-ur-Rahman, FRS; http://hdl.handle.net/11585/172882

الاتاحة: http://hdl.handle.net/11585/172882
https://doi.org/10.2174/9781608050291113060005

المؤلفون: M. Benaglia

المساهمون: K. Ding, Y. Uozumi, M. Benaglia

مصطلحات موضوعية: Catalyst immobilization, Catalyst recycle, Enantioselective catalysi, Organic catalysi, Recoverable catalyst, Stereoselective synthesis, Settore CHIM/06 - Chimica Organica

Relation: info:eu-repo/semantics/altIdentifier/isbn/9783527319138; ispartofbook:Handbook of asymmetric heterogeneous catalysis; firstpage:293; lastpage:322; alleditors:K. Ding, Y. Uozumi; http://hdl.handle.net/2434/59758; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84890995694

الاتاحة: http://hdl.handle.net/2434/59758
https://doi.org/10.1002/9783527623013.ch8

المؤلفون: Diego Savoia, Andrea Gualandi

المساهمون: Autta-ur-Rahman, FRS, Diego Savoia, Andrea Gualandi

مصطلحات موضوعية: aziridine ring opening, CHIRAL PERAZAMACROCYCLES, RADIOPHARMACEUTICALS, Acylic nucleophilic substitution, IMINES, MOLECULAR RECOGNITION, cyclam, METAL COMPLEX, ring closing metathesi, CYCLIZATION, aldol condensation, pseudopolypeptide, MOLECULAR KNOTS, ring closing, ASYMMETRIC SYNTHESIS, reductive coupling, mitsunobu reaction, atkins- richman procedure, molecular, NITROGEN LIGANDS, PERAZAMACROCYCLES, Amine, bridged macropolycycle, EPOXIDATION, ex-chiral pool synthesi, receptor (macrocyclic), alkyne-azide cycloaddition (click reaction), RING OPENING, CYCLOPHANE, guanidinium macrocycle, amide, superoxide dismutase mimic, CHIRAL STATIONARY PHASE, lactamization, REDUCTION, NUCLEOPHILIC SUBSTITUTION, cyclopolypeptide, MULTICOMPONENT REACTIONS, metal ion coordination, enantioselective catalysi, Henry reaction, on-resin synthesi, ENANTIOSELECTIVE RECOGNITION, SUPRAMOLECULAR CHEMISTRY, Ugi Reaction

وصف الملف: ELETTRONICO

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb429c6dc6ac652af58671445386bdb7
http://hdl.handle.net/11585/172882

المؤلفون: Companyó, Xavier, Viciano, Mónica, Rios, Ramon

المساهمون: Companyó, Xavier, Viciano, Mónica, Rios, Ramon

مصطلحات موضوعية: Enantioselective catalysi, Hydrogen bond, Organocatalysi, Supramolecular interaction, Organic Chemistry

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000274058200001; volume:7; issue:1; firstpage:1; lastpage:9; numberofpages:9; journal:MINI-REVIEWS IN ORGANIC CHEMISTRY; http://hdl.handle.net/11577/3268653; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-77949621592; http://www.benthamdirect.org/pages/b_viewarticle.php

الاتاحة: http://hdl.handle.net/11577/3268653
http://www.benthamdirect.org/pages/b_viewarticle.php

المؤلفون: V. Simonini, M. Benaglia, L. Pignataro, S. Guizzetti, G. Celentano

المساهمون: V. Simonini, M. Benaglia, L. Pignataro, S. Guizzetti, G. Celentano

مصطلحات موضوعية: Allyltrichlorosilane, Enantioselective catalysi, Homoallylic alcohol, N-oxide, Organocatalysis, Settore CHIM/06 - Chimica Organica

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000255644500027; volume:2008; issue:7; firstpage:1061; lastpage:1065; journal:SYNLETT; http://hdl.handle.net/2434/59787; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-42949174241

الاتاحة: http://hdl.handle.net/2434/59787
https://doi.org/10.1055/s-2008-1072509
http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-2008-1072509.pdf

المؤلفون: B. Lynikaite, J. Cvengros, C.M.A. Gennari, U. Piarulli

المساهمون: B. Lynikaite, J. Cvengro, U. Piarulli, C.M.A. Gennari

مصطلحات موضوعية: Asymmetric hydrogenation, Enantioselective catalysi, Phosphite, Rhodium, Settore CHIM/06 - Chimica Organica

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000253170200003; volume:49; issue:5; firstpage:755; lastpage:759; journal:TETRAHEDRON LETTERS; http://hdl.handle.net/2434/56610; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-37649025653

الاتاحة: http://hdl.handle.net/2434/56610
https://doi.org/10.1016/j.tetlet.2007.11.201

المؤلفون: SUPERCHI, Stefano, SCAFATO, Patrizia, ROSINI, Carlo, Lina Restaino

المساهمون: Superchi, Stefano, Scafato, Patrizia, Lina, Restaino, Rosini, Carlo

مصطلحات موضوعية: Asymmetric oxidation, Asymmetric synthesi, Chiral diol, Enantioselective catalysi, Sulfoxides

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000253555000042; volume:20; issue:3-4; firstpage:592; lastpage:596; numberofpages:5; journal:CHIRALITY; http://hdl.handle.net/11563/21421; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-39749142176

الاتاحة: http://hdl.handle.net/11563/21421
https://doi.org/10.1002/chir.20456

المؤلفون: F. Colombo, R. Annunziata, M. Benaglia

المساهمون: F. Colombo, R. Annunziata, M. Benaglia

مصطلحات موضوعية: Chiral catalyst, Chiral imine, Enantioselective catalysi, Homoallylic amine, Silver complex, Settore CHIM/06 - Chimica Organica

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000245706700008; volume:48; issue:15; firstpage:2687; lastpage:2690; journal:TETRAHEDRON LETTERS; http://hdl.handle.net/2434/36205; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-33947137197

الاتاحة: http://hdl.handle.net/2434/36205
https://doi.org/10.1016/j.tetlet.2007.02.071

المؤلفون: S. Orlandi, F. Colombo, M. Benaglia

المساهمون: S. Orlandi, F. Colombo, M. Benaglia

مصطلحات موضوعية: chiral bis-amine, copper complexe, propargylamine, enantioselective catalysi, acetylene addition, Settore CHIM/06 - Chimica Organica

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000230380900023; volume:2005; issue:10; firstpage:1689; lastpage:1692; journal:SYNTHESIS; http://hdl.handle.net/2434/16397; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-22244487956

الاتاحة: http://hdl.handle.net/2434/16397
https://doi.org/10.1055/s-2005-869896